Markus Weiler
Impact in
- Genetics top 0.5%
- Glioma Diagnosis and Treatment
- Neurogenetic and Muscular Disorders Research
- Cancer Research top 5%
- MicroRNA in disease regulation
- Cancer, Hypoxia, and Metabolism
Papers in
-
- Amyloidosis: Diagnosis, Treatment, Outcomes 14
- Epigenetics and DNA Methylation 4
- Genetics 30
- Glioma Diagnosis and Treatment 15
- Neurogenetic and Muscular Disorders Research 13
- Co-authors
- Wolfgang Wick (36 shared papers)Michael Weller (15 shared papers)Martin Bendszus (34 shared papers)Michael Platten (10 shared papers)Mirko Pham (12 shared papers)Sabine Heiland (25 shared papers)Andreas von Deimling (8 shared papers)Philipp Bäumer (10 shared papers)
- Journals
- Neurology (8 papers)European Journal of Neurology (7 papers)PLoS ONE (4 papers)Journal of Neurology (4 papers)Cancer Research (4 papers)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Markus Weiler
88 papers receiving 3.3k citations
Markus Weiler's Hit Papers
Peers
Comparison fields: 5 of 103
- Genetics 1.1k
- Cancer Research 432
- Oncology 582
- Neurology 295
- Radiology, Nuclear Medicine and Imaging 430
Countries citing papers authored by Markus Weiler
This map shows the geographic impact of Markus Weiler's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Markus Weiler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Markus Weiler more than expected).
Fields of papers citing papers by Markus Weiler
This network shows the impact of papers produced by Markus Weiler. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Markus Weiler. The network helps show where Markus Weiler may publish in the future.
Co-authors
The 25 scholars most cited alongside Markus Weiler, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 91 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | MGMT testing—the challenges for biomarker-based glioma treatment Hit paper breakdown → | 2014 | 402 |
| 2 | 2004 | 351 | |
| 3 | 2004 | 243 | |
| 4 | 2013 | 175 | |
| 5 | 2014 | 120 | |
| 6 | 2012 | 114 | |
| 7 | 2011 | 111 | |
| 8 | 2015 | 100 | |
| 9 | 2015 | 96 | |
| 10 | 2014 | 91 | |
| 11 | 2014 | 82 | |
| 12 | 2017 | 52 | |
| 13 | 2012 | 51 | |
| 14 | 2017 | 51 | |
| 15 | 2020 | 48 | |
| 16 | 2021 | 47 | |
| 17 | 2005 | 46 | |
| 18 | 2009 | 45 | |
| 19 | 2011 | 45 | |
| 20 | 2015 | 45 |
About Markus Weiler
Markus Weiler is a scholar working on Molecular Biology, Genetics, Oncology, Neurology and Pathology and Forensic Medicine, having authored 91 papers that have together received 3.3k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (15 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (14 papers), Neurogenetic and Muscular Disorders Research (13 papers), Cancer Treatment and Pharmacology (7 papers), Peripheral Nerve Disorders (5 papers), Epigenetics and DNA Methylation (4 papers), Multiple Sclerosis Research Studies (4 papers) and Trace Elements in Health (4 papers). The work is most often cited by research in Genetics (1.1k citations), Cancer Research (432 citations), Oncology (582 citations), Neurology (295 citations) and Radiology, Nuclear Medicine and Imaging (430 citations). Markus Weiler has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Wolfgang Wick, Michael Weller, Martin Bendszus, Michael Platten, Mirko Pham, Sabine Heiland, Andreas von Deimling, Philipp Bäumer, Jörg Wischhusen and Guido Reifenberger. Their work appears in journals such as Neurology, European Journal of Neurology, PLoS ONE, Journal of Neurology and Cancer Research.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.